Canonical Allele Identifier: CA118786
Gene: TCF7L2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7413
dbSNP Id: rs7903146

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112998590C>T , CM000672.2:g.112998590C>T GRCh38
NC_000010.10:g.114758349C>T , CM000672.1:g.114758349C>T GRCh37
NC_000010.9:g.114748339C>T NCBI36
NG_012631.1:g.53341C>T

Transcript Alleles

HGVS Amino-acid change
NM_001146274.1:c.450+33966C>T VV NP_001139746.1:p.=
NM_001146283.1:c.382-41435C>T VV NP_001139755.1:p.=
NM_001146284.1:c.382-41435C>T VV NP_001139756.1:p.=
NM_001146285.1:c.382-41435C>T VV NP_001139757.1:p.=
NM_001146286.1:c.382-41435C>T VV NP_001139758.1:p.=
NM_001198525.1:c.382-41435C>T VV NP_001185454.1:p.=
NM_001198526.1:c.382-41435C>T VV NP_001185455.1:p.=
NM_001198527.1:c.382-41435C>T VV NP_001185456.1:p.=
NM_001198528.1:c.382-41435C>T VV NP_001185457.1:p.=
NM_001198529.1:c.382-41435C>T VV NP_001185458.1:p.=
NM_001198530.1:c.381+46983C>T VV NP_001185459.1:p.=
NM_001198531.1:c.450+33966C>T VV NP_001185460.1:p.=
NM_030756.4:c.382-41435C>T VV NP_110383.2:p.=
XM_005270071.1:c.450+33966C>T XP_005270128.1:p.=
XM_005270073.1:c.450+33966C>T XP_005270130.1:p.=
XM_005270074.1:c.450+33966C>T XP_005270131.1:p.=
XM_005270075.1:c.450+33966C>T XP_005270132.1:p.=
XM_005270077.1:c.450+33966C>T XP_005270134.1:p.=
XM_005270078.1:c.450+33966C>T XP_005270135.1:p.=
XM_005270079.1:c.450+33966C>T XP_005270136.1:p.=
XM_005270080.1:c.382-41435C>T XP_005270137.1:p.=
XM_005270082.1:c.450+33966C>T XP_005270139.1:p.=
XM_005270083.1:c.450+33966C>T XP_005270140.1:p.=
XM_005270084.1:c.450+33966C>T XP_005270141.1:p.=
XM_005270085.1:c.450+33966C>T XP_005270142.1:p.=
XM_005270086.1:c.382-41435C>T XP_005270143.1:p.=
XM_005270088.1:c.382-41435C>T XP_005270145.1:p.=
XM_005270089.1:c.382-41435C>T XP_005270146.1:p.=
XM_005270091.2:c.450+33966C>T XP_005270148.1:p.=
XM_005270092.1:c.450+33966C>T XP_005270149.1:p.=
XM_005270093.1:c.450+33966C>T XP_005270150.1:p.=
XM_005270094.1:c.450+33966C>T XP_005270151.1:p.=
XM_005270095.1:c.450+33966C>T XP_005270152.1:p.=
XM_005270096.1:c.450+33966C>T XP_005270153.1:p.=
XM_005270100.1:c.450+33966C>T XP_005270157.1:p.=
XM_005270101.1:c.382-41435C>T XP_005270158.1:p.=
XM_005270102.1:c.450+33966C>T XP_005270159.1:p.=
XM_005270103.1:c.382-41435C>T XP_005270160.1:p.=
XM_005270104.1:c.382-41435C>T XP_005270161.1:p.=
XM_006717956.2:c.-10+33966C>T XP_006718019.1:p.=
XM_011540109.1:c.450+33966C>T XP_011538411.1:p.=
XM_011540110.1:c.382-41435C>T XP_011538412.1:p.=
XM_011540111.1:c.382-41435C>T XP_011538413.1:p.=
XM_011540112.1:c.450+33966C>T XP_011538414.1:p.=
XM_011540113.1:c.450+33966C>T XP_011538415.1:p.=
XM_011540114.1:c.450+33966C>T XP_011538416.1:p.=
XM_011540115.1:c.450+33966C>T XP_011538417.1:p.=
XM_011540116.1:c.450+33966C>T XP_011538418.1:p.=
XM_011540117.1:c.450+33966C>T XP_011538419.1:p.=
XM_011540118.1:c.450+33966C>T XP_011538420.1:p.=
XM_011540119.1:c.450+33966C>T XP_011538421.1:p.=
NM_001363501.1:c.450+33966C>T VV NP_001350430.1:p.=
XM_005270071.2:c.450+33966C>T XP_005270128.1:p.=
XM_005270075.2:c.450+33966C>T XP_005270132.1:p.=
XM_005270077.2:c.450+33966C>T XP_005270134.1:p.=
XM_005270078.2:c.450+33966C>T XP_005270135.1:p.=
XM_005270079.2:c.450+33966C>T XP_005270136.1:p.=
XM_005270080.2:c.382-41435C>T XP_005270137.1:p.=
XM_005270084.2:c.450+33966C>T XP_005270141.1:p.=
XM_005270085.2:c.450+33966C>T XP_005270142.1:p.=
XM_005270086.2:c.382-41435C>T XP_005270143.1:p.=
XM_005270088.2:c.382-41435C>T XP_005270145.1:p.=
XM_005270089.2:c.382-41435C>T XP_005270146.1:p.=
XM_005270091.3:c.450+33966C>T XP_005270148.1:p.=
XM_005270092.2:c.450+33966C>T XP_005270149.1:p.=
XM_005270093.3:c.450+33966C>T XP_005270150.1:p.=
XM_005270094.3:c.450+33966C>T XP_005270151.1:p.=
XM_005270095.2:c.450+33966C>T XP_005270152.1:p.=
XM_005270100.2:c.450+33966C>T XP_005270157.1:p.=
XM_005270101.3:c.382-41435C>T XP_005270158.1:p.=
XM_005270102.2:c.450+33966C>T XP_005270159.1:p.=
XM_005270103.2:c.382-41435C>T XP_005270160.1:p.=
XM_005270104.2:c.382-41435C>T XP_005270161.1:p.=
XM_011540109.2:c.450+33966C>T XP_011538411.1:p.=
XM_011540110.2:c.382-41435C>T XP_011538412.1:p.=
XM_011540111.2:c.382-41435C>T XP_011538413.1:p.=
XM_011540116.2:c.450+33966C>T XP_011538418.1:p.=
XM_017016584.2:c.450+33966C>T XP_016872073.1:p.=
XM_017016585.2:c.450+33966C>T XP_016872074.1:p.=
XM_017016586.2:c.450+33966C>T XP_016872075.1:p.=
XM_017016587.2:c.450+33966C>T XP_016872076.1:p.=
XM_017016588.2:c.382-41435C>T XP_016872077.1:p.=
XM_017016589.2:c.450+33966C>T XP_016872078.1:p.=
XM_017016590.2:c.450+33966C>T XP_016872079.1:p.=
XM_017016591.2:c.450+33966C>T XP_016872080.1:p.=
XM_017016592.2:c.450+33966C>T XP_016872081.1:p.=
XM_017016593.2:c.450+33966C>T XP_016872082.1:p.=
XM_017016594.2:c.382-41435C>T XP_016872083.1:p.=
XM_017016595.2:c.450+33966C>T XP_016872084.1:p.=
XM_017016596.2:c.450+33966C>T XP_016872085.1:p.=
XM_024448150.1:c.382-41435C>T XP_024303918.1:p.=
NM_001146274.2:c.450+33966C>T VV MANE Preferred NP_001139746.1:p.=
NM_001367943.1:c.450+33966C>T VV NP_001354872.1:p.=
ENST00000346198.5:n.291+33966C>T ENSP00000345640.4:p.=
ENST00000349937.6:c.450+33966C>T ENSP00000298692.4:p.=
ENST00000352065.9:c.382-41435C>T ENSP00000344823.5:p.=
ENST00000355717.8:c.382-41435C>T ENSP00000347949.4:p.=
ENST00000355995.8:c.450+33966C>T ENSP00000348274.4:p.=
ENST00000369395.5:c.382-41435C>T ENSP00000358402.1:p.=
ENST00000369397.8:c.382-41435C>T ENSP00000358404.4:p.=
ENST00000534894.5:c.381+46983C>T ENSP00000443626.2:p.=
ENST00000536810.5:c.382-41435C>T ENSP00000446238.2:p.=
ENST00000538897.5:c.450+33966C>T ENSP00000446172.1:p.=
ENST00000542695.5:c.64-41435C>T ENSP00000443883.2:p.=
ENST00000543371.5:c.450+33966C>T ENSP00000444972.2:p.=
ENST00000545257.5:c.382-41435C>T ENSP00000440547.2:p.=
ENST00000627217.2:c.450+33966C>T ENSP00000486891.1:p.=
ENST00000629706.2:n.382-41435C>T ENSP00000487507.1:p.=